Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10017305 0.925 0.120 4 10399599 intergenic variant T/C snv 0.26 1
rs10017335
LOC645513
0.925 0.040 4 119460368 intron variant C/G snv 0.28 2
rs10017573
STX18
0.925 0.040 4 4461337 intron variant T/C snv 0.15 2
rs10018902 4 120941346 intergenic variant G/A;T snv 1
rs10018951
TRAPPC11
1.000 0.080 4 183688220 intron variant C/T snv 0.18 1
rs10019193
LOC107986198 ; DDX60L ; PALLD
0.925 0.040 4 168526369 intron variant G/A;C snv 2
rs10019221
KCNIP4
4 21783741 intron variant G/C;T snv 1
rs10019259 1.000 0.040 4 95825984 intergenic variant C/A;T snv 1
rs10019567
LINC01378
1.000 0.040 4 117598351 intron variant T/C snv 0.23 1
rs10019681
FAM13A
4 88911381 intron variant C/T snv 0.28 2
rs10019835
GUCY1A1
1.000 0.120 4 155712034 intron variant T/A;C snv 1
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs1001989 8 106844987 intergenic variant T/C;G snv 1
rs10019997 4 136127444 intron variant C/T snv 0.47 1
rs10020288 1.000 0.040 4 28686220 intergenic variant G/A snv 0.38 2
rs10020323
NWD2
1.000 0.040 4 37448181 3 prime UTR variant G/A snv 0.23 1
rs10020457
PPARGC1A
1.000 0.040 4 23961338 intergenic variant G/A snv 0.31 1
rs10020574
LOC105374553
4 28061344 intergenic variant C/G snv 0.78 1
rs10021288 1.000 0.080 4 122084379 downstream gene variant G/A snv 0.21 1
rs10021465
FAM13A
4 88829210 intron variant A/G snv 0.37 2
rs10022002
PALLD
1.000 0.040 4 168563061 intron variant G/A snv 0.61 1
rs10022109
TET2
4 105166665 intron variant A/G snv 0.20 1
rs1002226 11 17384070 downstream gene variant C/T snv 0.69 1
rs10022462
PPM1K-DT
1.000 0.080 4 88322666 intron variant C/T snv 0.41 1
rs10023113
CAMK2D
1.000 0.080 4 113625548 intron variant A/G snv 0.18 1